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肿瘤新生抗原:从基础研究到临床应用。

Tumor neoantigens: from basic research to clinical applications.

机构信息

Department of Pulmonary Medicine, Shanghai Respiratory Research Institute, Zhongshan Hospital, Fudan University, Shanghai, China.

Department of Medical Oncology, Shanghai Pulmonary Hospital & Thoracic Cancer Institute, Tongji University School of Medicine, No. 507, Zheng Min Road, Shanghai, 200433, China.

出版信息

J Hematol Oncol. 2019 Sep 6;12(1):93. doi: 10.1186/s13045-019-0787-5.

Abstract

Tumor neoantigen is the truly foreign protein and entirely absent from normal human organs/tissues. It could be specifically recognized by neoantigen-specific T cell receptors (TCRs) in the context of major histocompatibility complexes (MHCs) molecules. Emerging evidence has suggested that neoantigens play a critical role in tumor-specific T cell-mediated antitumor immune response and successful cancer immunotherapies. From a theoretical perspective, neoantigen is an ideal immunotherapy target because they are distinguished from germline and could be recognized as non-self by the host immune system. Neoantigen-based therapeutic personalized vaccines and adoptive T cell transfer have shown promising preliminary results. Furthermore, recent studies suggested the significant role of neoantigen in immune escape, immunoediting, and sensitivity to immune checkpoint inhibitors. In this review, we systematically summarize the recent advances of understanding and identification of tumor-specific neoantigens and its role on current cancer immunotherapies. We also discuss the ongoing development of strategies based on neoantigens and its future clinical applications.

摘要

肿瘤新生抗原是真正的外来蛋白,完全不存在于正常的人类器官/组织中。它可以在主要组织相容性复合物 (MHC) 分子的背景下被新生抗原特异性 T 细胞受体 (TCR) 特异性识别。新出现的证据表明,新生抗原在肿瘤特异性 T 细胞介导的抗肿瘤免疫反应和成功的癌症免疫治疗中发挥着关键作用。从理论上讲,新生抗原是一种理想的免疫治疗靶点,因为它们与种系不同,可以被宿主免疫系统识别为非自身。基于新生抗原的治疗性个体化疫苗和过继性 T 细胞转移已显示出有前途的初步结果。此外,最近的研究表明,新生抗原在免疫逃逸、免疫编辑和对免疫检查点抑制剂的敏感性方面发挥着重要作用。在这篇综述中,我们系统地总结了对肿瘤特异性新生抗原的理解和鉴定的最新进展及其在当前癌症免疫治疗中的作用。我们还讨论了基于新生抗原的策略的最新发展及其未来的临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1bf/6731555/adcb688b086b/13045_2019_787_Fig1_HTML.jpg

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